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Elmar Medical Systems, Ltd.

Country not established

Devices
1

What Elmar Medical Systems, Ltd. makes

Elmar Medical Systems, Ltd. makes the CDS 2001 Artificial Kidney, a medical device designed for renal support therapy.

The CDS 2001 Artificial Kidney is classified as a Class II device and is listed in the FDA 510(k) registry; the company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Cds 2001 Artificial Kidney Ref K831376

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Elmar Medical Systems, Ltd. have in the registry?

The registry currently lists 1 device for Elmar Medical Systems, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Elmar Medical Systems, Ltd.'s devices?

Among its 1 most recently registered device, Elmar Medical Systems, Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Elmar Medical Systems, Ltd.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Elmar Medical Systems, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Elmar Medical Systems, Ltd. in the registry?

The most recently registered devices listed for Elmar Medical Systems, Ltd. include CDS 2001 ARTIFICIAL KIDNEY.

Generated automatically from registry data and not verified by a human reviewer.